Laboratory for Cheminformatics, Theory Department, National Institute of Chemistry, Hajdrihova 19, SI-1001 Ljubljana, Slovenia.
Chair of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Ljubljana, Aškerčeva 7, SI-1000 Ljubljana, Slovenia.
J Med Chem. 2020 Jun 11;63(11):5664-5674. doi: 10.1021/acs.jmedchem.9b01738. Epub 2020 Feb 17.
The emergence of bacterial resistance against life-saving medicines has forced the scientific community and pharmaceutical industry to take actions in the quest for novel antibacterials. These should not only overcome the existing bacterial resistance but also provide at least interim effective protection against emerging bacterial infections. Research into DNA gyrase and topoisomerase IV inhibitors has become a particular focus, with the description of a new class of bacterial topoisomerase type II inhibitors known as "novel bacterial topoisomerase inhibitors", NBTIs. Elucidation of the key structural modifications incorporated into these inhibitors and the impact these can have on their general physicochemical properties are detailed in this review. This defines novel bacterial topoisomerase inhibitors with promising antibacterial activities and potencies, which thus represent one potential example of the future "drugs for bad bugs", as identified by the World Health Organization.
细菌对抗救命药物的耐药性的出现迫使科学界和制药业采取行动,寻求新型抗菌药物。这些药物不仅要克服现有的细菌耐药性,还要对新出现的细菌感染提供至少暂时的有效保护。对 DNA 拓扑异构酶和拓扑异构酶 IV 抑制剂的研究成为一个特别关注的焦点,其中描述了一类新的细菌拓扑异构酶 II 抑制剂,称为“新型细菌拓扑异构酶抑制剂”(NBTI)。本文详细阐述了这些抑制剂中所包含的关键结构修饰及其对一般物理化学性质的影响。这一定义了具有潜在抗菌活性和效力的新型细菌拓扑异构酶抑制剂,因此代表了世界卫生组织确定的未来“针对有害细菌的药物”的一个潜在范例。